检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:张强[1] 边明艳 谭明旗[1] Zhang Qiang;Bian Mingyan;Tan Mingqi(Department of the Second Respiratory,Shengjing Hospital,China Medical University,Liaoning Shenyang 110000,China;Jinqiu Hospital of Liaoning Province,Liaoning Shenyang 110016,China.)
机构地区:[1]中国医科大学附属盛京医院第二呼吸内科,辽宁沈阳110000 [2]辽宁省金秋医院,辽宁沈阳110016
出 处:《现代肿瘤医学》2018年第17期2677-2682,共6页Journal of Modern Oncology
摘 要:目的:观察HA14-1及其联合顺铂对人小细胞肺癌NCI-H446细胞凋亡诱导作用并探讨其可能的作用机制,探讨其对Bcl-2、Bax表达的的影响。方法:选用人小细胞肺癌NCI-H446细胞株为研究对象,分为空白组、DDP组、HA14-1组及DDP+HA14-1组,分别作用24、48 h后,采用MTT法检测细胞抑制率,流式细胞仪检测细胞凋亡,Real time PCR法比较细胞内Bcl-2、Bax表达变化。结果:随着HA14-1及DDP浓度的增加,细胞抑制率逐渐增加,细胞凋亡率增高,联合用药组较单独用药组细胞的抑制率,凋亡率均增高,HA14-1作用细胞后,Bcl-2表达水平下降,Bax表达水平增高。结论:HA14-1可以诱导人小细胞肺癌凋亡,并增加肺癌细胞对DDP的化疗作用。Objective: To observe HA14-1 and HA14-1 combined cisplatin induced human small cell lung cancer NCI-H446 cell to apoptosis and explored its possible mechanism,affected the expression of Bcl-2,Bax.Methods: The human small cell lung cancer NCI-H446 cell line was the object of this study,which was divided into blank control group,DDP group,HA14-1 group and DDP + HA14-1 group,the role of 24 h,48 h,respectively,then cell inhibition rate were determined by MTT,the apoptotic rate of cells were measured by flow cytometry,the expression of intracellular Bcl-2,Bax gene were compared by Real time PCR. Results: With the increased concentrations of HA14-1 and DDP,cell inhibition rate increased gradually,the apoptotic rate was increased,the rate of cell inhibition and apoptosis of combination therapy group were higher than in the same dose group alone,HA14-1 roled in cells,Bcl-2 expression was lower,Bax expression was increased. Conclusion: HA14-1 could induce human small cell lung cancer apoptosis and increased the lung cancer cells to chemotherapy the role of DDP.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222